amoxicillin

Generic: amoxicillin

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler preferred pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amoxicillin 250 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8240
Product ID 68788-8240_8e79c23e-382b-4640-b0df-0e1cf42b6717
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065271
Listing Expiration 2027-12-31
Marketing Start 2022-08-09

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888240
Hyphenated Format 68788-8240

Supplemental Identifiers

RxCUI
308182
UNII
804826J2HU

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name amoxicillin (source: ndc)
Generic Name amoxicillin (source: ndc)
Application Number ANDA065271 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 21 CAPSULE in 1 BOTTLE (68788-8240-2)
  • 30 CAPSULE in 1 BOTTLE (68788-8240-3)
source: ndc

Packages (2)

Ingredients (1)

amoxicillin (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8e79c23e-382b-4640-b0df-0e1cf42b6717", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308182"], "spl_set_id": ["d6a33b28-f520-4a4c-b553-0ebd00558345"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (68788-8240-2)", "package_ndc": "68788-8240-2", "marketing_start_date": "20220809"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-8240-3)", "package_ndc": "68788-8240-3", "marketing_start_date": "20220809"}], "brand_name": "Amoxicillin", "product_id": "68788-8240_8e79c23e-382b-4640-b0df-0e1cf42b6717", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-8240", "generic_name": "Amoxicillin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/1"}], "application_number": "ANDA065271", "marketing_category": "ANDA", "marketing_start_date": "20220809", "listing_expiration_date": "20271231"}